Back to Search Start Over

Keloid-associated lymphoid tissues in keloid lesions express vitamin D receptor.

Authors :
Kilmister EJ
Lim KH
Itinteang T
van Schaijik B
Brasch HD
Davis PF
Tan ST
Source :
International journal of clinical and experimental pathology [Int J Clin Exp Pathol] 2019 Aug 01; Vol. 12 (8), pp. 3027-3031. Date of Electronic Publication: 2019 Aug 01 (Print Publication: 2019).
Publication Year :
2019

Abstract

Objectives: Vitamin D receptor (VDR) may play a role in keloid disorder. This study investigated the expression of VDR by the embryonic stem cell (ESC)-like population within keloid-associated lymphoid tissues (KALTs) which expresses components of the renin-angiotensin system (RAS). Methods: 11 formalin-fixed paraffin-embedded sections of keloid lesions (KLs) underwent 3,3-diaminobenzidine (DAB) immunohistochemical (IHC) staining for VDR. Immunofluorescence (IF) dual IHC staining of CD34/VDR and OCT4/VDR was performed on two representative KLs. Transcriptional activation of VDR was investigated in four representative snap-frozen KLs using reverse-transcriptase-quantitative polymerase chain reaction (RT-qPCR). Results: DAB IHC staining demonstrated the presence of VDR on the KALTs within the keloid tissue samples. RT-qPCR confirmed transcriptional activation of VDR. IF IHC staining demonstrated expression of VDR on the CD34 <superscript>+</superscript> and the OCT4 <superscript>+</superscript> endothelium of the microvessels, and the OCT4 <superscript>+</superscript> perivascular cells, within the KALTs. Conclusions: This study demonstrated the expression of VDR by the ESC-like population within the KALTs in KLs. Further work is needed to elucidate the precise interaction between VDR and the RAS in regulating the primitive population within the KALTs.<br />Competing Interests: TI, PD and ST are inventors of a PCT application Treatment of Fibrotic Conditions (PCT/NZ2016/050187). The authors are otherwise not aware of any commercial associations or financial relationships that might pose or create a conflict of interest with information presented in any submitted manuscript.<br /> (IJCEP Copyright © 2019.)

Details

Language :
English
ISSN :
1936-2625
Volume :
12
Issue :
8
Database :
MEDLINE
Journal :
International journal of clinical and experimental pathology
Publication Type :
Academic Journal
Accession number :
31934141